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| 008 | 100301s2006 xxu| s |||| 0|eng d | ||
| 020 | _a9780387449616 | ||
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_aRS420 _b.O685 2006 EB |
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_aOptimizing the zDrug-Likey Properties of Leads in Drug Discovery _cedited by Ronald T Borchardt, Edward H Kerns, Michael J Hageman, Dhiren R Thakker, James L Stevens |
| 260 |
_aNew York, NY _bSpringer International Publishing _c2006 |
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| 300 | _a1 recurso en línea (X, 512 p.) With CD-ROM. | ||
| 336 |
_aTexto (visual) _btxt _2rdacontent |
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| 337 |
_aelectrónico _bc _2rdamedia |
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| 338 |
_arecurso electrónico _bcr _2rdacarrier |
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| 338 |
_aonline resource _bcr _2rdacarrier |
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| 490 | 1 |
_aBiotechnology: Pharmaceutical Aspects _vIV |
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| 520 | _aDrug discovery and development is a very complex, costly, and ti- consuming process. Because of the uncertainties associated with predicting the pharmacological effects and the toxicity characteristics of new chemical entities in man, their clinical development is quite prone to failure. In recent years, phar- ceutical companies have come under increasing pressure to introduce new blockbuster drugs into the marketplace more rapidly. Companies have responded to these pressures by introducing new technologies and new strategies to expedite drug discovery and development. Drug discovery and development have traditionally been divided into three separate processes (i. e. , discovery research, preclinical development, and clinical development) that ideally should be integrated both organizationally and functionally. Instead, separate and distinct discovery research, preclinical development, and clinical development divisions were created within many companies during the 1980s and 1990s, Because of their isolation, scientists in the discovery research divisions often were advancing drug candidates into preclinical development that had marginal drug-like properties. For the purpose of this presentation, “drug-likeâ€{u0C32}operties refer to the moleculeâ€{u3830}hysicochemical, absorption-distribution-metabolism-excretion (ADME), and toxicological properties. Lacking optimal drug-like properties often caused these drug candidates to fail in preclinical or clinical development. | ||
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_2lcc _cLE |
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| 988 | _aEBOOK, EBSPRINGERrevisado | ||
| 650 | 7 |
_aMedicamentos _xDiseño _9395061 _0comprobar BNE20070512840 _2embne |
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| 700 | 1 |
_aBorchardt, Ronald T. _eeditor literario _0Local _984243 |
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| 700 | 1 |
_aKerns, Edward H. _eeditor literario _0Local _984244 |
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| 700 | 1 |
_aHageman, Michael J. _eeditor literario _0Local _984245 |
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| 700 | 1 |
_aThakker, Dhiren R _eeditor literario _984246 _0Local |
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| 700 | 1 |
_aStevens, James L _eeditor literario _984247 _0Local |
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| 856 | 4 | 0 |
_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-0-387-44961-6 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid) |
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_a.b12813230 _b10-10-17 _c01-10-14 |
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